HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653728Generated: October 30, 2026
Hydrochloric Acid → HCID 178494643, compound
https://huagongshe.com/reaction/653728
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 15654666 | HCID 15654666 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | HCID 178494643 | HCID 178494643 | 68% |
Reaction Steps
A mixture of methyl 1-[(2'-cyanobiphenyl-4-yl)methyl]-2-methoxymethylbenzimidazole-7-carboxylate (0.4 g) and trimethyltin azide (1.0 g) in toluene (10 ml) was refluxed for 49 hours. The reaction solution was concentrated to dryness to give a residue and the residue was dissolved in methanol (6 ml) and 1N-HCl (6 ml). The solution was allowed to stir for 3 hours and concentrated to dryness to give a residue. The residue was dissolved in CH2Cl2 -H2O and the mixture was made neutral with 1N-NaOH. The organic layer was washed with H2O, dried and concentrated to dryness to give a residue, which was purified by column chromatography on silica gel to give a crystalline product. Recrystallization from ethyl acetate-isopropylether gave colorless needles (0.3 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05128356 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-bf66b63d99e24b79b50aed19537785a9 |
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| Source note | uspto-grants-1992_07 |
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